Clinical Research Associate

• Assist in the preparation and coordination of clinical trial protocols and associated documents.
• Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out.
• Ensure that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements.
• Conduct site visits to assess the progress of clinical trials, monitor data accuracy, and ensure patient safety.
• Communicate with investigators and site staff to address issues or concerns related to the clinical trials.
• Assist in the review and management of clinical trial documentation, including case report forms (CRFs), informed consent forms, and regulatory submissions.
• Maintain study files and data to ensure compliance with applicable regulatory agencies.
• Support the clinical team in preparing reports, including monitoring reports and other regulatory documents.
• Attend and participate in internal meetings, as well as relevant training sessions, to develop knowledge and skills in clinical research.

Job Types: Full-time, Fresher

Pay: ₹22,869.01 - ₹38,019.71 per month

Benefits:

• Health insurance
• Paid sick time
• Provident Fund

Work Location: In person